HGVS | Genome Assembly |
---|---|
NC_000010.11:g.103086338G= , CM000672.2:g.103086338G= | GRCh38 |
NC_000010.10:g.104846095G= , CM000672.1:g.104846095G= | GRCh37 |
NC_000010.9:g.104836085G= | NCBI36 |
NG_042272.1:g.111969C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369878.9:c.*9158G= MANE Select | ENSP00000358894.3:n.*9158G= | |
ENST00000369878.8:c.*9158G= | ENSP00000358894.3:n.*9158G= | |
XR_001747118.1:n.12039G= | ||
XR_001747121.1:n.12003G= | ||
NM_017649.5:c.*9158G= MANE Select | NP_060119.3:n.*9158G= | |
NM_199076.3:c.*9158G= | NP_951058.1:n.*9158G= |